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7-OXO-7H-BENZIMIDAZO[2,1-A]BENZ[DE]ISOQUINOLINE-3-CARBOXYLIC ACID ACETATE

7-OXO-7H-BENZIMIDAZO[2,1-A]BENZ[DE]ISOQUINOLINE-3-CARBOXYLIC ACID ACETATE Structure
  • ₹29850
  • Product name: 7-OXO-7H-BENZIMIDAZO[2,1-A]BENZ[DE]ISOQUINOLINE-3-CARBOXYLIC ACID ACETATE
  • CAS: 52029-86-4
  • MF: C19H10N2O3
  • MW: 314.29
  • EINECS:
  • MDL Number:MFCD06411456
  • Synonyms:STO-609;STO-609 ACETIC ACID;7-Oxo-7H-benzimidazo[2,1-a]benz[de]isoquinoline-3-carboxylic acid - acetic acid;7-Oxo-7H-benzimidazo[2,1-a]benz[de]isoquinoline-3-carboxylic Acid;7H-BENZ[DE]BENZIMIDAZO[2,1-A]ISOQUINOLINE-7-ONE-3-CARBOXYLIC ACID, ACETATE;7-OXO-7H-BENZIMIDAZO[2,1-A]BENZ[DE]ISOQUINOLINE-3-CARBOXYLIC ACID ACETATE;STO-609, >98%;STO609;STO 609
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Brand

  • Sigma-Aldrich(India)

Package

  • 5MG
  • ManufacturerSigma-Aldrich(India)
  • Product number570250
  • Product descriptionSTO-609 - CAS 52029-86-4 - Calbiochem A cell-permeable and reversible naphthoyl fused benzimidazole compound that acts as a highly selective, potent, ATP-competitive inhibitor of Ca2+/CaM-
  • Packaging5MG
  • Price₹29850
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich(India) 570250 STO-609 - CAS 52029-86-4 - Calbiochem A cell-permeable and reversible naphthoyl fused benzimidazole compound that acts as a highly selective, potent, ATP-competitive inhibitor of Ca2+/CaM- 5MG ₹29850 2022-06-14 Buy

Properties

Melting point :>300 °C
Boiling point :716.9±62.0 °C(Predicted)
Density :1.54±0.1 g/cm3(Predicted)
storage temp. :Sealed in dry,2-8°C
solubility :DMSO: 15 mg/mL at ≥60 °C
form :solid
pka :2.65±0.20(Predicted)
color :Light yellow to yellow

Safety Information

Symbol(GHS):
Signal word:
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
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Description

STO-609 is a naphthoyl fused benzimidazole cell-permeable compound. It is known to be a very potent and selective ATP-competitive CaMKK inhibitor. STO-609 has been shown to bind to the CaMKK catalytic domain, thus inhibiting autophosphorylation. STO-609 has not been found to significantly affect the activities of MLCK, CaMKII, CaMKI, CaMKIV, PKC, PKA, or p42 MAP kinase. It has been observed to inhibit AMP-activated protein kinase phosphorylation. STO-609 is an inhibitor of CaMKK α and CaMKK β and an activator of aryl hydrocarbon receptor.

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